Canonical Allele Identifier: CA3272602

Gene: MAP3K1

Linked Data

• dbSNP Id: rs746479827
• ExAC: 5:56155654 G / A
• gnomAD v2: 5-56155654-G-A
• gnomAD v3: 5-56859827-G-A
• gnomAD v4: 5-56859827-G-A
• COSMIC: COSM3344759
• MyVariant Identifiers: chr5:g.56155654G>A (hg19) ; chr5:g.56859827G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859827G>A , CM000667.2:g.56859827G>A	GRCh38
NC_000005.9:g.56155654G>A , CM000667.1:g.56155654G>A	GRCh37
NC_000005.8:g.56191411G>A	NCBI36
NG_031884.1:g.49755G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.746G>A MANE Select	ENSP00000382423.3:p.Arg249His
ENST00000399503.3:c.746G>A	ENSP00000382423.3:p.Arg249His
NM_005921.1:c.746G>A	NP_005912.1:p.Arg249His
XM_005248519.3:c.368G>A	XP_005248576.2:p.Arg123His
XM_011543406.1:c.491G>A	XP_011541708.1:p.Arg164His
XM_011543407.1:c.746G>A	XP_011541709.1:p.Arg249His
XM_011543408.1:c.746G>A	XP_011541710.1:p.Arg249His
XM_017009484.1:c.335G>A	XP_016864973.1:p.Arg112His
XM_017009485.1:c.257G>A	XP_016864974.1:p.Arg86His
XR_001742068.2:n.777G>A
NM_005921.2:c.746G>A MANE Select	NP_005912.1:p.Arg249His